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July 1, 2020 - Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices and Certain Devices Requiring Direct Marking: Immediately in Effect Guidance for Industry and Food and Drug Administration Staff June 30, 2020 - Development and Licensure of Vaccines to Prevent COVID-19: Guidance for Industry: FDA is issuing this guidance to assist sponsors in the clinical development and licensure of vaccines for the prevention of COVID-19. June 29, 2020 - Review and Update of Device Establishment Inspection Processes and Standards: Guidance for Industry: FDA is issuing this draft guidance to comply with section 702(b)(1) of the FDA Reauthorization Act of 2017 (FDARA) (Public Law 115-52), which directs FDA to issue draft guidance that specifies how the Agency will implement uniform processes and standards that are applicable to inspections ( other than for-cause) of foreign and domestic medical device establishments.  June 29, 2020 - Development of Anti-Infective Drug Products for the Pediatric Population : Draft Guidance for Industry: The purpose of this guidance is to provide general recommendations on the development of anti-infective drug products for the pediatric population.

For a more comprehensive list of all official FDA Guidance Documents and other regulatory guidances, please visit here.